28192-55-4

Upstream product

• 148139-26-8 2-(tribromotelluro)benzaldehyde 
• 28192-54-3 2-(butyldichlorotelluro)benzaldehyde 
• 18982-54-2 o-bromobenzyl alcohol 
• 28192-52-1 2-(butyltelluro)benzaldehyde 
• 28192-51-0 2-(butyltelluro)benzaldehyde diethyl acetal 
• 35822-58-3 2-bromobenzaldehyde diethyl acetal 
• 6630-33-7 ortho-bromobenzaldehyde 
• 34824-58-3 2-(2-bromophenyl)-1,3-dioxolan 

Downstream Products

• 130191-41-2 di<2-(2',4',6'-trimethylphenyl)iminomethinyl>phenyl ditelluride 
• 130216-65-8 di<2-(4'-iodophenyl)iminomethinyl>phenyl ditelluride 
• 28192-21-4 C₇H₅Cl₃OTe 
• 1515875-34-9 dipyrromethane ditelluride 
• 125508-98-7 bis<2-(hydroxyiminomethyl)phenyl> ditelluride 
• 130191-42-3 di(2-tert-butyliminomethinyl)phenyl ditelluride 
• 130191-40-1 di<2-(4'-methoxylphenyl)iminomethinyl>phenyl ditelluride 
• 121272-49-9 di<2-(4'-methylphenyl)iminomethinyl>phenyl ditelluride 

Relevant academic research and scientific papers

Synthesis and structural characterisation of the aggregates of benzo-1,2-chalcogenazole 2-oxides

Iodine oxidation of bis[2-(hydroxyiminomethyl)phenyl] dichalcogenides yields benzo-1,2-chalcogenazole 2-oxides. Annulated derivatives of iso-tellurazole N-oxides spontaneously aggregate into cyclic tetra- and hexamers through Te?O chalcogen bonding; the s

5H-1,2-OXATELLUROLES AND THEIR BENZO ANALOGS: SYNTHESIS AND REACTIONS

Tetracoordinated derivatives of 2-halo-2-aryl-5H-1,2-oxatelluroles and 1-halo-1-butyl-3H-benz-2,1-oxatelluroles were synthesized by the oxidation of 3-aryltelluro-2-propen-1-ols and the dehydrogenation of 2-butyldihalotellurobenzyl alcohols.The halogen at